US3101999A - Low temperature defluorination of phosphate material - Google Patents
Low temperature defluorination of phosphate material Download PDFInfo
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- US3101999A US3101999A US82383A US8238361A US3101999A US 3101999 A US3101999 A US 3101999A US 82383 A US82383 A US 82383A US 8238361 A US8238361 A US 8238361A US 3101999 A US3101999 A US 3101999A
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- Prior art keywords
- triple superphosphate
- temperature
- alkaline earth
- fluorine
- fluorine content
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B25/00—Phosphorus; Compounds thereof
- C01B25/16—Oxyacids of phosphorus; Salts thereof
- C01B25/26—Phosphates
- C01B25/32—Phosphates of magnesium, calcium, strontium, or barium
- C01B25/328—Defluorination during or after the preparation
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/20—Inorganic substances, e.g. oligoelements
- A23K20/26—Compounds containing phosphorus
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S426/00—Food or edible material: processes, compositions, and products
- Y10S426/807—Poultry or ruminant feed
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S71/00—Chemistry: fertilizers
- Y10S71/03—Defluorination
Definitions
- This invention relates to the preparation of solid phosphates useful as animal feed supplements. More partic ularly, it relates to the defluorination of triple superphosphate by controlled temperature calcination. Still more specifically, the invention is concerned with the defluorination of triple superphosphate by controlled temperature calcination followed by an alkaline earth metal fusion of the s c-calcined products to obtain phosphates nutritionally valuable as animal feed supplements.
- triple superphosphate containing of from about 1% to 3% fluorine is subjected to heat treatment at temperatures within the range of from about 1050 F. to about 1300 F.
- the fluorine content is reduced substantially within this controlled temperature range.
- the so-calcined, defluorinated phosphate mixture can next undergo fusion by heat treatment with an alkaline material, such as alkali metal carbonate or an alkaline earth oxide, to form phosphates useful as nutritionally valuable animal feed supplements.
- an alkaline material such as alkali metal carbonate or an alkaline earth oxide
- calcination is preferably carried out in a rotary kiln calciner, whereby the surface of the'triple' superphosphate is exposed for the ready removal of flu-, orine and occluded water.
- Resultant products obtained from calcining crude triple superphosphate, are believed to be mixed, water-insoluble, dehydrated phosphates. latter can then be fused with an alkaline material, such as either an alkaline earth oxide or a mixture of alkaline earth oxide and an alkali metal carbonate, to obtain principally either tricalcium orthophosphate or dicalcium monosodium orthophosphate.
- the defiuori-nation operation of the present invention can be carried out at relatively low temperatures, usually between 1050' F. and 1300* F; A preferred operating temperature for effecting the initial calcination is one between 1100 F. and 1200 F.
- calcination may also be carried out in the presence of from 1% to 5% added clay, talc or diatomaceous earth. Further modifications are also contemplated.
- Resultant mixed, dehydrated, water-insoluble phospirates so obtained contain, as far as is known, a mixture of dicalcium pyrophosphate, calcium acid pyrophosphate, calcium metaphosphate and polymeric calcium phosphates in a variety of crystalline forms. Further, the fluorine content therein is about 0.26 percent or lower, being reduced from approximately 2.5 percent fluorine and the phosphorus content expressed as P 0 is increased from 47% P 0 of the original charge to about 60% P 0 in the final calcined product.
- the defluorinated, mixed, dehydrated phosphates cannot be immediately em ployed as an animal feed supplement, for the reason that they are not nutritionally available to the animal. Accordingly, the calcined products must be further proc essed to convert them into a more useful and desirable form.
- the calcined phosphate mixture can be further processed by subjecting such admixture to fusion with alkaline materials. Fusion occurs at temperatures between 1800" F. and 2000 F. within from five to sixty minutes. Tribasic orthophosphates are readily recovered in yields of percent or better.
- Illustrative alklaline treating materials are: alkali metal carbonates, such as sodium carbonate, potassium carbonate and alkaline earth carbonates or oxides, such as calcium carbonate or calcium oxide, as well as mixtures thereof such as sodium carbonate and calcium oxide, preferably present in equimolar amounts.
- alkali metal carbonates such as sodium carbonate, potassium carbonate and alkaline earth carbonates or oxides, such as calcium carbonate or calcium oxide, as well as mixtures thereof such as sodium carbonate and calcium oxide, preferably present in equimolar amounts.
- Example 1 Triple superphosphate (previously prepared by: admixing 1.6 parts of 54% P 0 wet process phosphoric acid a with one part of finely ground phosphate rock [80% of which passes through a 200 mesh Tyler screen and containing about 34% P and allowing it to cure for forty days) is a friable product, which on analysis contains approximately 47% P 0 and a high fluorine content, namely about 2.2% fluorine in the form of metal fluorides, silicon fluorides and hydrogen fluoride.
- the latter triple superphosphate is added in finely divided form to a rotary kiln to which 5% diatomaceous earth is added. The kiln contents are heated to a temperature between about 1050 F. and 1100 F. for about thirty minutes.
- the so-calcined product is next removed from the rotary kiln. On analysis it is found to contain about 59% P 0 and about 0.25% fluorine.
- the calcined material which is a mixed, dehydrated calcium phosphate, is converted into essentially tricalcium orthophosphate.
- the phosphorus can readily be absorbed nutritionally by animals, such as chickens.
- Example 2 Five parts of triple superphosphate, as defined in Example 1 above, are admixed with 0.25 part of diatomaceous earth and the mixture is added to a rotary kiln. Water vapor is added continuously to the internal kiln atmosphere. The contents therein are heated to a temperature of 1150' F. and maintained at that temperature fora period of one-half hour. On analysis, the fluorine content of the calcined triple superphosphate is found to be reduced from 2.26% to 0.15%, while simultaneously observing an increase in the P 0 content from 47% to 59%.
- the so-calcined product Four parts of the so-calcined product are admixed and ground with one part of calcium oxide and heated in a direct fired kiln to a temperature of 1800 F. for about 15 minutes.
- the calcined material which is a mixed, dehydrated calcium phosphate, is converted into essentially tricalcium orthophosphate.
- the phosphorus can be readily absorbed nutritionally by animals, such as chickens.
- Example 3 The procedure of Example 2 is repeated in every detail except that calcium oxide is replaced by a mixture consisting of 0.5 part of calcium oxide and 0.75 part of sodium carbonate per part 'of calcium oxide used therein.
- X-ray diffraction analysis shows the product to consist principally of tribasic calcium sodium orthophosphate and tricalciu-m orthophosphate.
- Example 4 Repeating Example 1 in every detail except that the initial calcining temperature is 1300 F. Similar fluorine content reduction is thereby obtained.
- an improved process for preparing phosphatic animal feed supplement of high nutritional availability which comprises: heat treating triple superphosphate containing more than 1% fluorine at a temperature between about 1050 F. and 1300 F. for a time suflicient to eflfect the reduction of the fluorine content of said triple superphosphate to less than about 0.26%, calcining the latter defluorinated triple superphosphate product at a temperature of fromabout 1800- F. to about 2000 F. in the presence of an alkaline material selected from the group consisting of alkali metal carbonates, alkaline earth carbonates, alkaline earth oxides and mixtures thereof, for from about five to sixty minutes, and thereafter recovering nutritionally available animal feed phosphates of low fluorine content.
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- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
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- Organic Chemistry (AREA)
- Animal Husbandry (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Fodder In General (AREA)
Description
United States Patent "ice No Drawing. Filed Jan. 13, 1961, Ser. No. 82,383 3 Claims. (Cl. 23-408) This invention relates to the preparation of solid phosphates useful as animal feed supplements. More partic ularly, it relates to the defluorination of triple superphosphate by controlled temperature calcination. Still more specifically, the invention is concerned with the defluorination of triple superphosphate by controlled temperature calcination followed by an alkaline earth metal fusion of the s c-calcined products to obtain phosphates nutritionally valuable as animal feed supplements.
Attempts have heretofore been made to produce nutritionally valuable animal food supplements from superphosphates or triple super-phosphates by various techniques. Unfortunately, none is entirely commercially satisfactory. For instance, triple superphosphate has been subjected to heat treatment to remove its fluorine content. Calcining temperatures in excess of 1700 F., usually in the range of 2000 F. to 3000 F., are employed to reduce the aforementioned fluorine content to approximately one-half percent or below. Unfortunately, the use of elevated tempenatures, i.e., temperatures above 1700 F., has the major drawback that it requires large fuel consumption and results in the evolution of copious quantities of noxious sulfur dioxide gas. The latter is discharged directly into the atmosphere. This practice is undesirable because the atmosphere becomes polluted. The chemical absorption of sulfur dioxide gas on the large scale is an expensive and troublesome operation. To obviate this and other drawbacks, attempts have been made to defluorinate a superphosphate involving, for example, a sulfuric 'acid leach followed by the removal of the solids so-formed and the heat treatment of the residual solution. The leaching step appears to produce removable and undesirable impurities which interfere with the subsequent heat-treating operation; however, this leach step entails an additional operation which renders the over-all process economically unfeasible. The desirability for providing an over-all economical process for the manufacture of nutritionally valuable phosphates is well established. If such a process can be developed, it would be highly desirable.
It is, therefore, a principal object of the present invention to provide defluorinated, dehydrated phosphates capable of ready conversion to satisfactory sources of phosphorus for animal nutrition. It is a further object to provide defluorinated, mixed, dehydrated phosphates prepared by calcination at temperatures substantially below 1700 F. It is still a further object to economically prepare solid phosphates in nutritionally available form. Other objects and advantages will become apparent from a consideration of the following detailed description.
To this end, triple superphosphate containing of from about 1% to 3% fluorine is subjected to heat treatment at temperatures within the range of from about 1050 F. to about 1300 F. Unexpectedly, the fluorine content is reduced substantially within this controlled temperature range. The so-calcined, defluorinated phosphate mixture can next undergo fusion by heat treatment with an alkaline material, such as alkali metal carbonate or an alkaline earth oxide, to form phosphates useful as nutritionally valuable animal feed supplements.
According to the process of the present invention,
3,191,999 Patented Aug. 27, 1963 2 triple superphosphate as prepared, for instance, by in'ti mately contacting phosphate rock and wet process phosphoric acid and curing the mixture for approximately forty days, is calcined at temperatures between about 1050 F. and about 1300" F. Usually, ten minutes and not more than about one hour are sufficient to cause substantial defiuorination to occur. Thus, the fluorine content is almost quantitatively reduced.
In general, calcination is preferably carried out in a rotary kiln calciner, whereby the surface of the'triple' superphosphate is exposed for the ready removal of flu-, orine and occluded water. Resultant products, obtained from calcining crude triple superphosphate, are believed to be mixed, water-insoluble, dehydrated phosphates. latter can then be fused with an alkaline material, such as either an alkaline earth oxide or a mixture of alkaline earth oxide and an alkali metal carbonate, to obtain principally either tricalcium orthophosphate or dicalcium monosodium orthophosphate. 7
It is advantageous that the defiuori-nation operation of the present invention can be carried out at relatively low temperatures, usually between 1050' F. and 1300* F; A preferred operating temperature for effecting the initial calcination is one between 1100 F. and 1200 F. However, to facilitate the defluorinati'on operation by prevent ing sticking or agglomeration of the triple superphosphate, calcination may also be carried out in the presence of from 1% to 5% added clay, talc or diatomaceous earth. Further modifications are also contemplated. For instance, maintaining a water vapor atmosphere in the presence of added clay or diatomaceous earth is also desirable to increase the rate of fluorine evolution; Mixed water-insoluble dehydrated phosphates containing a mol ratio of phosphorus to fluorine of 100 to 1 or better are obtained.
Resultant mixed, dehydrated, water-insoluble phospirates so obtained contain, as far as is known, a mixture of dicalcium pyrophosphate, calcium acid pyrophosphate, calcium metaphosphate and polymeric calcium phosphates in a variety of crystalline forms. Further, the fluorine content therein is about 0.26 percent or lower, being reduced from approximately 2.5 percent fluorine and the phosphorus content expressed as P 0 is increased from 47% P 0 of the original charge to about 60% P 0 in the final calcined product. However, the defluorinated, mixed, dehydrated phosphates cannot be immediately em ployed as an animal feed supplement, for the reason that they are not nutritionally available to the animal. Accordingly, the calcined products must be further proc essed to convert them into a more useful and desirable form.
Advantageously, the calcined phosphate mixture can be further processed by subjecting such admixture to fusion with alkaline materials. Fusion occurs at temperatures between 1800" F. and 2000 F. within from five to sixty minutes. Tribasic orthophosphates are readily recovered in yields of percent or better.
Illustrative alklaline treating materials are: alkali metal carbonates, such as sodium carbonate, potassium carbonate and alkaline earth carbonates or oxides, such as calcium carbonate or calcium oxide, as well as mixtures thereof such as sodium carbonate and calcium oxide, preferably present in equimolar amounts.
The invention will be illustrated in conjunction with the following examples which are to be taken as illustrative only and not by way of limitation. All parts are by weight, unless otherwise noted.
Example 1 Triple superphosphate (previously prepared by: admixing 1.6 parts of 54% P 0 wet process phosphoric acid a with one part of finely ground phosphate rock [80% of which passes through a 200 mesh Tyler screen and containing about 34% P and allowing it to cure for forty days) is a friable product, which on analysis contains approximately 47% P 0 and a high fluorine content, namely about 2.2% fluorine in the form of metal fluorides, silicon fluorides and hydrogen fluoride. The latter triple superphosphate is added in finely divided form to a rotary kiln to which 5% diatomaceous earth is added. The kiln contents are heated to a temperature between about 1050 F. and 1100 F. for about thirty minutes. The so-calcined product is next removed from the rotary kiln. On analysis it is found to contain about 59% P 0 and about 0.25% fluorine.
Four pants of the so-calcined product are admixed and ground with one part of calcium oxide and heated in a direct fired kiln to a temperature of 1800 F. for about 15 minutes. The calcined material, which is a mixed, dehydrated calcium phosphate, is converted into essentially tricalcium orthophosphate. In this form, the phosphorus can readily be absorbed nutritionally by animals, such as chickens.
Example 2 Five parts of triple superphosphate, as defined in Example 1 above, are admixed with 0.25 part of diatomaceous earth and the mixture is added to a rotary kiln. Water vapor is added continuously to the internal kiln atmosphere. The contents therein are heated to a temperature of 1150' F. and maintained at that temperature fora period of one-half hour. On analysis, the fluorine content of the calcined triple superphosphate is found to be reduced from 2.26% to 0.15%, while simultaneously observing an increase in the P 0 content from 47% to 59%.
Four parts of the so-calcined product are admixed and ground with one part of calcium oxide and heated in a direct fired kiln to a temperature of 1800 F. for about 15 minutes. The calcined material which is a mixed, dehydrated calcium phosphate, is converted into essentially tricalcium orthophosphate. In this form, the phosphorus can be readily absorbed nutritionally by animals, such as chickens.
4 Example 3 The procedure of Example 2 is repeated in every detail except that calcium oxide is replaced by a mixture consisting of 0.5 part of calcium oxide and 0.75 part of sodium carbonate per part 'of calcium oxide used therein. X-ray diffraction analysis shows the product to consist principally of tribasic calcium sodium orthophosphate and tricalciu-m orthophosphate.
Example 4 Repeating Example 1 in every detail except that the initial calcining temperature is 1300 F. Similar fluorine content reduction is thereby obtained.
We claim:
1. In an improved process for preparing phosphatic animal feed supplement of high nutritional availability the improvement which comprises: heat treating triple superphosphate containing more than 1% fluorine at a temperature between about 1050 F. and 1300 F. for a time suflicient to eflfect the reduction of the fluorine content of said triple superphosphate to less than about 0.26%, calcining the latter defluorinated triple superphosphate product at a temperature of fromabout 1800- F. to about 2000 F. in the presence of an alkaline material selected from the group consisting of alkali metal carbonates, alkaline earth carbonates, alkaline earth oxides and mixtures thereof, for from about five to sixty minutes, and thereafter recovering nutritionally available animal feed phosphates of low fluorine content.
2. The process according to claim 1, in which the alkaline earth oxide is calcium oxide.
3. The process according to claim 1, in which the alkaline earth compound and alkali metal carbonate mixture consists of calcium oxide and sodium carbonate, respectively.
References Cited in the file of this patent UNITED STATES PATENTS 1,880,491 Rothe et al Oct. 4, 1932 2,234,511 Wight et a1. Mar. 11, 1941 2,442,969 Butt June 8, 1948 2,562,718 Hollingsworth July 31, 1951
Claims (1)
1. IN AN IMPROVED PROCESS FOR PREPARING PHOSPHATIC ANINAL FEED SUPPLEMENT OF HIGH NUTRITONAL AVAILABILITY THE IMPROVEMENT WHICH COMPRISES: HEAT TREATING TRIPLE SUPERPHOSPHATE CONTAINING MORE THAN 1% FLUORINE AT A TEMPERATURE BETWEEN ABOUT 1050*F. AND 1300*F. FOR TIME SUFFICIENT TO EFFECT THE REDUCTION OF THE FLUORINE CONTENT OF SAID TRIPLE SUPERPHOSPHATE TO LESS THAN ABOUT 0.26%, CALCINING THE LATTER DEFLUORINATED TRIPLE SUPERPHOSPHATE PRODUCT AT A TEMPERATURE OF FROM ABOUT 1800*F. TO ABOUT 2000*F. IN THE PRESENCE OF AN ALKALINE MATERIAL SELECTED FROM THE GROUP CONSISTING OF ALKALI METAL CARBONATES, ALKALINE EARTH CARBONATES, ALKALINE EARTH OXIIDES AND MIXTURES THEREOF, FOR FROM ABOUT FIVE TO SIXTY MINUTES, AND THEREAFTER RECOVERING NUTRITONALLY AVAILABLE ANIMAL FEED PHOSPHATES OF LOW FLUORINE CONTENT.
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US82383A US3101999A (en) | 1961-01-13 | 1961-01-13 | Low temperature defluorination of phosphate material |
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US82383A US3101999A (en) | 1961-01-13 | 1961-01-13 | Low temperature defluorination of phosphate material |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3189433A (en) * | 1962-06-11 | 1965-06-15 | Borden Co | Method of agglomerating phosphate material |
US3207580A (en) * | 1962-04-13 | 1965-09-21 | American Cyanamid Co | Preparation of wet process phosphoric acid |
US3658549A (en) * | 1968-07-23 | 1972-04-25 | Karl Geiersberger | Calcium sodium phosphate feed supplements |
US3931416A (en) * | 1973-08-11 | 1976-01-06 | Chemische Fabrik Kalk Gmbh | Process for manufacturing calcium-sodium-phosphate consisting mainly of Rhenanit and suitable for use as supplementary animal food |
FR2446254A1 (en) * | 1979-01-15 | 1980-08-08 | Ugine Kuhlmann | DEFLUORED NATURAL CALCIUM PHOSPHATE FOR ANIMAL FEED |
US4716026A (en) * | 1986-01-22 | 1987-12-29 | International Minerals & Chemical Corp. | Defluorination kiln restriction control agent and method |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1880491A (en) * | 1927-11-23 | 1932-10-04 | Firm Kali Chemie Ag | Producing calcined phosphates |
US2234511A (en) * | 1938-03-05 | 1941-03-11 | Davison Chemical Corp | Animal feed supplement and process of manufacture |
US2442969A (en) * | 1946-05-16 | 1948-06-08 | Int Minerals & Chem Corp | Manufacture of defluorinated tricalcium phosphate |
US2562718A (en) * | 1947-10-18 | 1951-07-31 | Coronet Phosphate Company | Defluorination of phosphate rock |
-
1961
- 1961-01-13 US US82383A patent/US3101999A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1880491A (en) * | 1927-11-23 | 1932-10-04 | Firm Kali Chemie Ag | Producing calcined phosphates |
US2234511A (en) * | 1938-03-05 | 1941-03-11 | Davison Chemical Corp | Animal feed supplement and process of manufacture |
US2442969A (en) * | 1946-05-16 | 1948-06-08 | Int Minerals & Chem Corp | Manufacture of defluorinated tricalcium phosphate |
US2562718A (en) * | 1947-10-18 | 1951-07-31 | Coronet Phosphate Company | Defluorination of phosphate rock |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3207580A (en) * | 1962-04-13 | 1965-09-21 | American Cyanamid Co | Preparation of wet process phosphoric acid |
US3189433A (en) * | 1962-06-11 | 1965-06-15 | Borden Co | Method of agglomerating phosphate material |
US3658549A (en) * | 1968-07-23 | 1972-04-25 | Karl Geiersberger | Calcium sodium phosphate feed supplements |
US3931416A (en) * | 1973-08-11 | 1976-01-06 | Chemische Fabrik Kalk Gmbh | Process for manufacturing calcium-sodium-phosphate consisting mainly of Rhenanit and suitable for use as supplementary animal food |
FR2446254A1 (en) * | 1979-01-15 | 1980-08-08 | Ugine Kuhlmann | DEFLUORED NATURAL CALCIUM PHOSPHATE FOR ANIMAL FEED |
US4716026A (en) * | 1986-01-22 | 1987-12-29 | International Minerals & Chemical Corp. | Defluorination kiln restriction control agent and method |
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